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pro vyhledávání: '"Varadrajulu G. Mandiri"'
Autor:
Kailas D. Datkhile, Kshamata V. Thorat ,, Madhavi N. Patil, Rohit D. Vhaval, Varadrajulu G. Mandiri
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 04, Iss 02, Pp 70-80 (2015)
Background: Duchenne muscular dystrophy is the most common neuromuscular disease of childhood caused by deletion or point mutations in the dystrophin gene. Though the importance of deletion mutations in the dystrophin gene causing DMD have been r
Externí odkaz:
https://doaj.org/article/e11ae292290848d085208320a9002567
